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Variant : CV555416 (GRCh37/hg19 15q26.2-26.3(chr15:98144229-99857338)x1) Homo sapiens

Symbol: CV555416
Name: GRCh37/hg19 15q26.2-26.3(chr15:98144229-99857338)x1
Condition: not provided [RCV000683721]
Clinical Significance: likely pathogenic
Last Evaluated: 11/16/2017
Review Status: no assertion criteria provided
Related Genes: ARRDC4   FAM169B   IGF1R   LRRC28   PGPEP1L   SYNM   TTC23  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.9:g.(?_98144229)_(99857338_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh371598,144,229 - 99,857,338CLINVAR
Cytogenetic Map1515q26.2-26.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13797433
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-08-06
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.